Wonchae Choe

4.6k total citations · 1 hit paper
89 papers, 3.6k citations indexed

About

Wonchae Choe is a scholar working on Molecular Biology, Epidemiology and Cell Biology. According to data from OpenAlex, Wonchae Choe has authored 89 papers receiving a total of 3.6k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Molecular Biology, 15 papers in Epidemiology and 14 papers in Cell Biology. Recurrent topics in Wonchae Choe's work include Metabolism, Diabetes, and Cancer (20 papers), Signaling Pathways in Disease (14 papers) and Endoplasmic Reticulum Stress and Disease (12 papers). Wonchae Choe is often cited by papers focused on Metabolism, Diabetes, and Cancer (20 papers), Signaling Pathways in Disease (14 papers) and Endoplasmic Reticulum Stress and Disease (12 papers). Wonchae Choe collaborates with scholars based in South Korea, United States and Vietnam. Wonchae Choe's co-authors include Joohun Ha, Insug Kang, Sung Soo Kim, Judith L. Campbell, Kyung‐Sik Yoon, Martin E. Budd, Minjung Kim, Hee Yun, Young Taek Oh and Jung Yeon Lee and has published in prestigious journals such as Nucleic Acids Research, Journal of Biological Chemistry and Molecular and Cellular Biology.

In The Last Decade

Wonchae Choe

88 papers receiving 3.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Heat Shock Response and Heat Shock Proteins: Current Understanding and Future Opportunities in Human Diseases

2024 65 citations Manish Kumar Singh, Yoonhwa Shin et al. International Journal of Molecular Sciences profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Wonchae Choe South Korea	36	2.2k	486	471	379	323	89	3.6k
Sun Sik Bae South Korea	37	2.8k 1.2×	499 1.0×	532 1.1×	454 1.2×	418 1.3×	120	4.5k
Xiuwen Tang China	32	2.8k 1.2×	388 0.8×	254 0.5×	344 0.9×	265 0.8×	70	4.2k
Paul Nioi United States	17	3.1k 1.4×	328 0.7×	438 0.9×	271 0.7×	225 0.7×	33	4.3k
Duan‐Fang Liao China	30	2.2k 1.0×	734 1.5×	348 0.7×	272 0.7×	349 1.1×	120	3.9k
Long Chen China	34	1.7k 0.7×	331 0.7×	356 0.8×	483 1.3×	204 0.6×	127	3.9k
Tao Su China	35	1.7k 0.8×	441 0.9×	299 0.6×	272 0.7×	418 1.3×	125	3.6k
Christopher J.B. Nicol Canada	32	2.4k 1.1×	552 1.1×	901 1.9×	668 1.8×	431 1.3×	75	4.0k
Hong‐Seob So South Korea	39	2.1k 0.9×	413 0.8×	337 0.7×	343 0.9×	513 1.6×	119	4.4k
Maddalena Fratelli Italy	33	2.7k 1.2×	413 0.8×	526 1.1×	261 0.7×	584 1.8×	89	4.8k
Pengfei Wu China	36	2.2k 1.0×	824 1.7×	685 1.5×	288 0.8×	293 0.9×	107	4.0k

Countries citing papers authored by Wonchae Choe

Since Specialization

Citations

This map shows the geographic impact of Wonchae Choe's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Wonchae Choe with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Wonchae Choe more than expected).

Fields of papers citing papers by Wonchae Choe

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Wonchae Choe. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Wonchae Choe. The network helps show where Wonchae Choe may publish in the future.

Co-authorship network of co-authors of Wonchae Choe

This figure shows the co-authorship network connecting the top 25 collaborators of Wonchae Choe. A scholar is included among the top collaborators of Wonchae Choe based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Wonchae Choe. Wonchae Choe is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Singh, Manish Kumar, Yoonhwa Shin, Songhyun Ju, et al.. (2024). Heat Shock Response and Heat Shock Proteins: Current Understanding and Future Opportunities in Human Diseases. International Journal of Molecular Sciences. 25(8). 4209–4209. 65 indexed citations breakdown →

Jang, Jiwon, Wonchae Choe, Kyung‐Sik Yoon, et al.. (2023). Molecular Mechanisms of Neuroprotection by Ketone Bodies and Ketogenic Diet in Cerebral Ischemia and Neurodegenerative Diseases. International Journal of Molecular Sciences. 25(1). 124–124. 39 indexed citations

Liu, Wenpeng, Piotr Polaczek, Yuan Meng, et al.. (2023). FANCD2 and RAD51 recombinase directly inhibit DNA2 nuclease at stalled replication forks and FANCD2 acts as a novel RAD51 mediator in strand exchange to promote genome stability. Nucleic Acids Research. 51(17). 9144–9165. 13 indexed citations

Choe, Wonchae, et al.. (2022). Beta-naphthoflavone and doxorubicin synergistically enhance apoptosis in human lung cancer cells by inducing doxorubicin accumulation, mitochondrial ROS generation, and JNK pathway signaling. Biochemical and Biophysical Research Communications. 635. 37–45. 2 indexed citations

Akter, Salima, Md. Ataur Rahman, Mohammad Nazmul Hasan, et al.. (2022). Recent Advances in Ovarian Cancer: Therapeutic Strategies, Potential Biomarkers, and Technological Improvements. Cells. 11(4). 650–650. 62 indexed citations

Kim, Kiyoon, et al.. (2021). 2-O-Methylhonokiol Suppresses HCV Replication via TRAF6-Mediated NF-kB Activation. International Journal of Molecular Sciences. 22(12). 6499–6499. 6 indexed citations

Suh, Kwang Sik, Eun Mi Choi, Hyunsook Kim, et al.. (2018). Xanthohumol ameliorates 2,3,7,8‐tetrachlorodibenzo‐p‐dioxin–induced cellular toxicity in cultured MC3T3‐E1 osteoblastic cells. Journal of Applied Toxicology. 38(7). 1036–1046. 6 indexed citations

Yang, Goowon, Jihyun Lee, Sangsu Lee, et al.. (2016). Krill Oil Supplementation Improves Dyslipidemia and Lowers Body Weight in Mice Fed a High-Fat Diet Through Activation of AMP-Activated Protein Kinase. Journal of Medicinal Food. 19(12). 1120–1129. 20 indexed citations

Jeong, Kwon, Seong‐Jin Kim, Byung Su Kwon, et al.. (2014). p53 negatively regulates Pin1 expression under ER stress. Biochemical and Biophysical Research Communications. 454(4). 518–523. 14 indexed citations

10.

Chung, Sung Hyun, Jong‐Seok Lim, Wonchae Choe, et al.. (2012). Quercetin enhances hypoxia-mediated apoptosis via direct inhibition of AMPK activity in HCT116 colon cancer. APOPTOSIS. 17(9). 938–949. 74 indexed citations

11.

Park, In Ja, Min Jung Kim, Ock Jin Park, et al.. (2011). Cryptotanshinone induces ER stress-mediated apoptosis in HepG2 and MCF7 cells. APOPTOSIS. 17(3). 248–257. 73 indexed citations

12.

Park, Chang-Eun, Hee Yun, Byung-Il Min, et al.. (2010). The Antioxidant Effects of Genistein Are Associated with AMP-Activated Protein Kinase Activation and PTEN Induction in Prostate Cancer Cells. Journal of Medicinal Food. 13(4). 815–820. 88 indexed citations

13.

Yun, Hee, Jong‐Hwa Lee, Chang-Eun Park, et al.. (2009). Inulin Increases Glucose Transport in C2C12 Myotubes and HepG2 Cells via Activation of AMP-Activated Protein Kinase and Phosphatidylinositol 3-Kinase Pathways. Journal of Medicinal Food. 12(5). 1023–1028. 22 indexed citations

14.

Oh, Young Taek, Jung Yeon Lee, Jinhwa Lee, et al.. (2009). Oleic acid reduces lipopolysaccharide-induced expression of iNOS and COX-2 in BV2 murine microglial cells: Possible involvement of reactive oxygen species, p38 MAPK, and IKK/NF-κB signaling pathways. Neuroscience Letters. 464(2). 93–97. 107 indexed citations

15.

Yoon, Hana, Young Taek Oh, Ji Hyun Choi, et al.. (2008). Activation of AMP-activated protein kinase by kainic acid mediates brain-derived neurotrophic factor expression through a NF-kappaB dependent mechanism in C6 glioma cells. Biochemical and Biophysical Research Communications. 371(3). 495–500. 37 indexed citations

16.

Choi, Kyu Jin, Min Jin Lim, Jin Hwan Kim, et al.. (2007). Overexpressed Cyclophilin A in Cancer Cells Renders Resistance to Hypoxia- and Cisplatin-Induced Cell Death. Cancer Research. 67(8). 3654–3662. 122 indexed citations

17.

Jhun, Bong Sook, Jung Yeon Lee, Young Taek Oh, et al.. (2006). Inhibition of AMP-activated protein kinase suppresses IL-2 expression through down-regulation of NF-AT and AP-1 activation in Jurkat T cells. Biochemical and Biophysical Research Communications. 351(4). 986–992. 21 indexed citations

18.

Lee, Jung Yeon, Bong Sook Jhun, Young Taek Oh, et al.. (2005). Activation of adenosine A3 receptor suppresses lipopolysaccharide-induced TNF-α production through inhibition of PI 3-kinase/Akt and NF-κB activation in murine BV2 microglial cells. Neuroscience Letters. 396(1). 1–6. 129 indexed citations

19.

Hoopes, Laura L. Mays, Martin E. Budd, Wonchae Choe, Tao Weitao, & Judith L. Campbell. (2002). Mutations in DNA Replication Genes Reduce Yeast Life Span. Molecular and Cellular Biology. 22(12). 4136–4146. 52 indexed citations

20.

Budd, Martin E., Wonchae Choe, & Judith L. Campbell. (2000). The Nuclease Activity of the Yeast Dna2 Protein, Which Is Related to the RecB-like Nucleases, Is Essential in Vivo. Journal of Biological Chemistry. 275(22). 16518–16529. 125 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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